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Improving Predictability of Food-Drug and Drug-Drug Interaction Risks by Utilizing In Vitro Simulated Gastrointestinal Dissolution Model for High-Risk Oral Drug Products (U01) Clinical Trial Optional
Due: Apr 8, 2024
HHS-FDA
$250,000
Description
The purpose of this funding opportunity is to examine the utility of an in vitro simulated gastrointestinal (GI) dissolution model for the assessment of in vitro performance of amorphous solid dispersion (ASD) drug products under different clinically relevant conditions. The goal is to develop and validate the in vitro mechanistic methodology to provide an improved understanding of impact of food and acid reducing agents on the absorption for test and reference listed drug (RLD) drug products, taking into consideration their pote...
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Estimated Total Program Funding
$250,000
Expected Number of Awards
2
Award Ceiling
$250,000
Eligible Applicants
- State governments
- County governments
- City or township governments
- Special district governments
- Independent school districts
- Public and State controlled institutions of higher education
- Native American tribal governments (Federally recognized)
- Public housing authorities/Indian housing authorities
- Native American tribal organizations (other than Federally recognized tribal governments)
- Nonprofits having a 501 (c) (3) status with the IRS, other than institutions of higher education
- Nonprofits that do not have a 501 (c) (3) status with the IRS, other than institutions of higher education
- Private institutions of higher education
- For-profit organizations other than small businesses
- Small businesses
- Unrestricted
Funding Type
Cooperative Agreement
Categories of Funding Activity
- Agriculture
- Consumer Protection
- Food and Nutrition
Opportunity Type
Discretionary
Grantor Contact Information
terrin.brown@fda.hhs.gov
Other Grantor Informaiton
Terrin Brown Grantor
Additional information
RFA-FD-24-009 Funding Opportunity Announcement
Supporting Link
https://grants.nih.gov/grants/guide/rfa-files/RFA-FD-24-009.html
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